Canonical Allele Identifier: CA2650532221

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218405077-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405079del , CM000663.2:g.218405079del	GRCh38
NC_000001.10:g.218578421del , CM000663.1:g.218578421del	GRCh37
NC_000001.9:g.216645044del	NCBI36
NG_027721.1:g.64746del
NG_027721.2:g.64746del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.347-90del MANE Select	ENSP00000355897.4:n.347-90del
ENST00000366929.4:c.431-90del	ENSP00000355896.4:n.431-90del
ENST00000366930.8:c.347-90del	ENSP00000355897.4:n.347-90del
ENST00000488793.1:n.11-90del
NM_001135599.2:c.431-90del	NP_001129071.1:n.431-90del
NM_003238.3:c.347-90del	NP_003229.1:n.347-90del
NM_001135599.3:c.431-90del	NP_001129071.1:n.431-90del
NM_003238.4:c.347-90del	NP_003229.1:n.347-90del
NR_138148.1:n.1765-90del
NR_138149.1:n.1849-90del
NM_003238.5:c.347-90del	NP_003229.1:n.347-90del
NM_003238.6:c.347-90del MANE Select	NP_003229.1:n.347-90del
NM_001135599.4:c.431-90del	NP_001129071.1:n.431-90del
NR_138148.2:n.1713-90del
NR_138149.2:n.1797-90del